Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		304 122 85 0.21 20 0.12
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia 		246 45 33 8.4E-02 10 0.10
CUI: C0002902
Disease: Anencephaly
Anencephaly 		59 10 22 0.10 6 9.2E-02
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		76 15 9 3.7E-02 6 8.6E-02
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		688 40 41 5.0E-02 7 7.4E-02
CUI: C1536220
Disease: ST segment elevation myocardial infarction
ST segment elevation myocardial infarction 		264 16 13 3.0E-02 5 6.9E-02
CUI: C0810364
Disease: Cleft Lip with or without Cleft Palate
Cleft Lip with or without Cleft Palate 		99 50 19 7.3E-02 7 6.7E-02
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		3 5 2 1.1E-02 4 6.5E-02
CUI: C0220810
Disease: Congenital defects
Congenital defects 		126 6 15 5.2E-02 4 6.3E-02
CUI: C0035067
Disease: Renal Artery Stenosis
Renal Artery Stenosis 		37 8 7 3.3E-02 4 6.2E-02
CUI: C1853238
Disease: Conotruncal defect
Conotruncal defect 		51 45 11 5.0E-02 6 6.0E-02
CUI: C0042847
Disease: Vitamin B 12 Deficiency
Vitamin B 12 Deficiency 		29 11 5 2.5E-02 4 5.9E-02
CUI: C0278877
Disease: Adult Meningioma
Adult Meningioma 		405 30 29 5.2E-02 5 5.8E-02
CUI: C1762616
Disease: Meningioma, benign, no ICD-O subtype
Meningioma, benign, no ICD-O subtype 		404 30 28 5.0E-02 5 5.8E-02
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		85 13 6 2.3E-02 4 5.7E-02
CUI: C0011269
Disease: Dementia, Vascular
Dementia, Vascular 		212 32 22 6.0E-02 5 5.7E-02
CUI: C1392786
Disease: Cognitive changes
Cognitive changes 		50 15 4 1.8E-02 4 5.6E-02
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity 		202 16 12 3.3E-02 4 5.5E-02
CUI: C0025281
Disease: Meniere Disease
Meniere Disease 		69 36 6 2.5E-02 5 5.4E-02
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome 		669 77 36 4.4E-02 7 5.3E-02
CUI: C0013537
Disease: Eclampsia
Eclampsia 		241 38 20 5.0E-02 5 5.3E-02
CUI: C4275242
Disease: Sudden sensorineural hearing loss
Sudden sensorineural hearing loss 		72 38 8 3.3E-02 5 5.3E-02
CUI: C0013080
Disease: Down Syndrome
Down Syndrome 		766 80 37 4.1E-02 7 5.2E-02
CUI: C0025286
Disease: Meningioma
Meningioma 		634 43 41 5.3E-02 5 5.1E-02
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		537 45 26 3.8E-02 5 5.0E-02